A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597557



Internal ID21546173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1807015..1811558hg38UCSC Ensembl
chr11:1828245..1832788hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384544
hg194544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073835
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597557
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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